Publicação:
Expression and processing of recombinant sarafotoxins precursor in Pichia pastoris

dc.contributor.authorBorgheresi, RAMB
dc.contributor.authorPalma, Mario Sergio [UNESP]
dc.contributor.authorDucancel, F.
dc.contributor.authorCamargo, ACM
dc.contributor.authorCarmona, E.
dc.contributor.institutionInstituto Butantan
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionCEA Saclay
dc.date.accessioned2014-05-20T13:54:28Z
dc.date.available2014-05-20T13:54:28Z
dc.date.issued2001-08-01
dc.description.abstractSarafotoxins are peptides isolated from the Atractaspisw snake venom. with strong constrictor effect on cardiac and smooth muscle. They are structurally and functionally related to endothelins. The sarafotoxins precursor cDNA predicts an unusual structure 'rosary-type', with 12 successive similar stretches of sarafotoxin (SRTX) and spacer, in the present work, the recombinant precursor of SRTXs was sub-cloned and expressed in the yeast Pichia pastoris. and secreted to the culture medium, Characterization by SDS-PAGE, immunoblot, mass spectrometry and biological activity, suggests that intact precursor was expressed but processing into mature toxins also occurred. Furthermore, our results indicate that the correct proportion of sarafotoxin types as contained in the precursor, is obtained in the yeast culture medium. Contractile effects of the expressed toxins, on rat and Bothrops jararaca isolated aorta, were equivalent to 5 X 10(-10) M and 5 x 10(-11) M of sarafotoxin b, respectively. The enzymes responsible for the complete maturation of sarafotoxins precursor are still unknown. Our results strongly suggest that the yeast Pichia pastoris is able to perform such a maturation process. Thus, the yeast Pichia pastoris may offer an alternative to snake venom gland to tentatively identify the molecular process responsible for SRTXs release. (C) 2001 Elsevier B.V. Ltd. All rights reserved.en
dc.description.affiliationInst Butantan, Farmacol Lab, BR-05503900 São Paulo, Brazil
dc.description.affiliationInst Butantan, Lab Bioquim & Biofis, BR-05503900 São Paulo, Brazil
dc.description.affiliationUNESP, IBRC, CEIS, Lab Biol Estrutural & Zooquim, São Paulo, Brazil
dc.description.affiliationCEA Saclay, Dept Ingenierie & Etud Prot, F-91191 Gif Sur Yvette, France
dc.description.affiliationUnespUNESP, IBRC, CEIS, Lab Biol Estrutural & Zooquim, São Paulo, Brazil
dc.format.extent1211-1218
dc.identifierhttp://dx.doi.org/10.1016/S0041-0101(00)00265-8
dc.identifier.citationToxicon. Oxford: Pergamon-Elsevier B.V., v. 39, n. 8, p. 1211-1218, 2001.
dc.identifier.doi10.1016/S0041-0101(00)00265-8
dc.identifier.issn0041-0101
dc.identifier.lattes2901888624506535
dc.identifier.urihttp://hdl.handle.net/11449/19471
dc.identifier.wosWOS:000168881200011
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofToxicon
dc.relation.ispartofjcr2.352
dc.relation.ispartofsjr0,692
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.subjectsarafotoxinspt
dc.subjectprecursor of safarotoxinspt
dc.subjectprocessing enzymespt
dc.subjectexpression in Pichia pastorispt
dc.titleExpression and processing of recombinant sarafotoxins precursor in Pichia pastorisen
dc.typeArtigo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
dspace.entity.typePublication
unesp.author.lattes2901888624506535
unesp.author.orcid0000-0002-7363-8211[2]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Rio Claropt
unesp.departmentBiologia - IBpt

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